Orbital Disease (ORBIT)

Alias:
Orbit
Orbital Diseases
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Orbital Disease, also known as orbit, is related to graves disease 1 and graves ophthalmopathy, and has symptoms including eye manifestations and visual disturbance. An important gene associated with Orbital Disease is TSHR (Thyroid Stimulating Hormone Receptor), and among its related pathways/superpathways are Innate Immune System and Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell. The drugs Ciprofloxacin and Cytochrome P-450 Enzyme Inhibitors have been mentioned in the context of this disorder. Affiliated tissues include eye and ciliary ganglion, and related phenotypes are immune system and hematopoietic system
Related ID:
MESH:D009916
ICD11:73394252

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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21
171
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Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Related Drugs

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Disease Model

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MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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